Evidence map›Paper›PMID 30851191›Full record

ArticleThe British journal of dermatology2019

Conjunctivitis in dupilumab clinical trials.

B Akinlade, E Guttman-Yassky, M de Bruin-Weller, E L Simpson, A Blauvelt, M J Cork, E Prens, P Asbell, E Akpek, J Corren and 18 more

Open access · bronzeAbstract read
In one paragraph

Article in The British journal of dermatology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 158 papers, 9 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
158citing papers in PubMed, 9 pooled it
46.9field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

158 citing papers in PubMed, 9 syntheses or guidelines pooled it, 411 citations in OpenAlex.

  1. Pooled it
  2. Biomarkers for therapeutic response and adverse outcomes in atopic dermatitis: A systematic review.Journal of the European Academy of Dermatology and Venereology : JEADV · 2026
    Pooled it
  3. European Guideline (EuroGuiDerm) on atopic eczema: Living update.Journal of the European Academy of Dermatology and Venereology : JEADV · 2025
    Guideline
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98 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

28 authors at 16 institutions in 7 countries.

B AkinladeRegeneron Pharmaceuticals, Inc., Tarrytown, NY, U.S.A.ORCID 0000-0003-2334-5717
E Guttman-YasskyDepartment of Dermatology, Icahn School of Medicine at Mount Sinai Medical Center, New York, NY, U.S.A.ORCID 0000-0002-9363-324X
M de Bruin-WellerDepartment of Dermatology & Allergology, University Medical Center Utrecht, Utrecht, the Netherlands.ORCID 0000-0002-1249-6993
E L SimpsonDepartment of Dermatology, Oregon Health & Science University, Portland, OR, U.S.A.
A BlauveltOregon Medical Research Center, Portland, OR, U.S.A.ORCID 0000-0002-2633-985X
M J CorkSheffield Dermatology Research, Department of Infection, Immunity and Cardiovascular Disease, The University of Sheffield Medical School, Sheffield, U.K.
E PrensDepartment of Dermatology, Erasmus MC, Rotterdam, the Netherlands.
P AsbellHamilton Eye Institute, University of Tennessee Health Science Center, Memphis, TN, U.S.A.
E AkpekWilmer Eye Institute at Johns Hopkins University School of Medicine, Baltimore, MD, U.S.A.
J CorrenDavid Geffen School of Medicine at UCLA, Los Angeles, CA, U.S.A.
C BachertENT Department, Ghent University Hospital, Ghent, Belgium.
I HiranoNorthwestern University Feinberg School of Medicine, Chicago, IL, U.S.A.
J WeyneRegeneron Pharmaceuticals, Inc., Tarrytown, NY, U.S.A.
A KorotzerRegeneron Pharmaceuticals, Inc., Tarrytown, NY, U.S.A.
Z ChenRegeneron Pharmaceuticals, Inc., Tarrytown, NY, U.S.A.
T HultschSanofi Genzyme, Cambridge, MA, U.S.A.
X ZhuRegeneron Pharmaceuticals, Inc., Tarrytown, NY, U.S.A.
J D DavisRegeneron Pharmaceuticals, Inc., Tarrytown, NY, U.S.A.
L MannentSanofi R&D, Chilly-Mazarin, France.
J D HamiltonRegeneron Pharmaceuticals, Inc., Tarrytown, NY, U.S.A.
A TeperSanofi, Bridgewater, NJ, U.S.A.
H StaudingerSanofi, Bridgewater, NJ, U.S.A.
E RizovaSanofi Genzyme, Cambridge, MA, U.S.A.
G PirozziSanofi, Bridgewater, NJ, U.S.A.
N M H GrahamRegeneron Pharmaceuticals, Inc., Tarrytown, NY, U.S.A.
B ShumelRegeneron Pharmaceuticals, Inc., Tarrytown, NY, U.S.A.
M ArdeleanuRegeneron Pharmaceuticals, Inc., Tarrytown, NY, U.S.A.
A WollenbergLudwig-Maximilian University, Munich, Germany.
Regeneron (United States) · USSanofi (United States) · USGenesys (United States) · USErasmus MC · NLGhent University Hospital · BEJohns Hopkins University · USLudwig-Maximilians-Universität München · DEMount Sinai Medical Center · USNorthwestern University · USOregon Health & Science University · USOregon Medical Research Center · USSanofi (France) · FRUniversity Medical Center Utrecht · NLUniversity of California, Los Angeles · USUniversity of Sheffield · GBUniversity of Tennessee Health Science Center · US

Funding

Regeneron Pharmaceuticals, IncSanofi
6 · The paper itself

Abstract

backgroundDupilumab blocks the shared receptor component for interleukin (IL)-4 and IL-13. It is approved in the U.S.A. for patients aged ≥ 12 years with moderate-to-severe atopic dermatitis (AD) uncontrolled by topical prescription medicines or who cannot use topical medicines, for patients in Japan whose AD is uncontrolled with existing therapies, for patients with moderate-to-severe AD in Europe who are candidates for systemic therapy and for patients aged ≥ 12 years for maintenance treatment of moderate-to-severe asthma uncontrolled with their current medicines. AD trials have reported increased incidence of conjunctivitis for dupilumab vs. placebo.

objectivesTo characterize further the occurrence and risk factors of conjunctivitis in dupilumab clinical trials.

methodsWe evaluated randomized placebo-controlled trials of dupilumab in AD (n = 2629), asthma (n = 2876), chronic rhinosinusitis with nasal polyps (CRSwNP) (n = 60) and eosinophilic oesophagitis (EoE) (n = 47).

resultsIn most AD trials, dupilumab-treated patients had higher conjunctivitis incidence than placebo controls. Higher baseline AD severity and previous history of conjunctivitis were associated with increased conjunctivitis incidence. Conjunctivitis was mostly mild to moderate. Most cases recovered or resolved during the treatment period; two patients permanently discontinued dupilumab due to conjunctivitis or keratitis. Common treatments included ophthalmic corticosteroids, antibiotics, and antihistamines or mast cell stabilizers. Most cases were diagnosed by the investigators. In asthma and CRSwNP trials, the incidence of conjunctivitis was lower for both dupilumab and placebo than in AD trials; dupilumab did not increase the incidence compared with placebo. In the EoE trial, no patients had conjunctivitis.

conclusionsConjunctivitis was more frequent with dupilumab treatment in most AD trials. In dupilumab trials in other type 2 diseases, incidence of conjunctivitis was overall very low, and was similar for dupilumab and placebo. In AD, the incidence of conjunctivitis was associated with AD severity and prior history of conjunctivitis. The aetiology and treatment of conjunctivitis in dupilumab-treated patients require further study. What's already known about this topic? Ocular disorders, including allergic conjunctivitis, are common in patients with atopic dermatitis (AD). In most dupilumab AD trials, dupilumab-treated patients had higher conjunctivitis incidence than those receiving placebo. Most cases were mild to moderate and recovered or were recovering during study treatment; study treatment discontinuation due to conjunctivitis was rare. Conjunctivitis incidence was very low and similar for dupilumab and placebo in clinical trials in asthma, chronic rhinosinusitis with nasal polyps and eosinophilic oesophagitis. What does this study add? This analysis confirms and extends the results of the individual clinical trials. Baseline disease-related factors, including AD severity, prior conjunctivitis history and certain biomarkers (thymus and activation-regulated chemokine, IgE, eosinophils), were associated with increased incidence of conjunctivitis. Patients who responded well to dupilumab had reduced incidence of conjunctivitis. Further study is needed to elucidate the aetiology and treatment of conjunctivitis in dupilumab-treated patients with AD.

Indexed as

AdultAntibodies, Monoclonal, HumanizedAsthmaConjunctivitisDermatitis, AtopicEosinophilic EsophagitisHumansIncidenceInterleukin-4 Receptor alpha SubunitNasal PolypsPlacebosRandomized Controlled Trials as TopicRhinitisRisk FactorsSeverity of Illness IndexSinusitisAntibodies, Monoclonal, HumanizeddupilumabIL4R protein, humanInterleukin-4 Receptor alpha SubunitPlacebos

Identifiers

PMID30851191
PMCPMC6850316
OpenAlexW2921132618

What OpenQuestion holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.